Advancing small cell lung cancer metastasis research: innovations in preclinical mouse models.

IF 8.7
Qiqi Zhao, Liang Hu, Hongbin Ji
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Abstract

Small cell lung cancer (SCLC) represents one of the most aggressive malignancies, featured with its extraordinary metastatic capacity. Preclinical mouse models have become indispensable systems for studying the molecular mechanisms underlying SCLC metastasis. This review summarizes recent advances in genetically engineered mouse models (GEMMs) and transplantation models for SCLC metastasis research, highlighting their unique advantages in investigating oncogenic drivers, tumor heterogeneity, immune interactions, and therapeutic responses. We further discuss emerging technologies capable of integrating with these models to advance both mechanistic and translational research. Lineage tracing and multi-omics approaches have provided unprecedented resolution in mapping clonal dynamics and phenotypic plasticity during SCLC metastasis. High-throughput in vivo screening has accelerated the systematic identification of novel metastasis regulators, and humanized mouse models offer clinically relevant systems for investigating human-specific tumor-immune interactions and supporting preclinical evaluation of immunotherapies. Collectively, these preclinical systems are reshaping our understanding of SCLC metastasis and providing powerful platforms to guide therapeutic discovery.

推进小细胞肺癌转移研究:临床前小鼠模型的创新。
小细胞肺癌(SCLC)是最具侵袭性的恶性肿瘤之一,具有非凡的转移能力。临床前小鼠模型已成为研究SCLC转移的分子机制不可或缺的系统。本文综述了用于SCLC转移研究的基因工程小鼠模型(GEMMs)和移植模型的最新进展,强调了它们在研究致癌驱动因素、肿瘤异质性、免疫相互作用和治疗反应方面的独特优势。我们进一步讨论了能够与这些模型集成的新兴技术,以推进机械和转化研究。谱系追踪和多组学方法为SCLC转移过程中克隆动力学和表型可塑性的绘制提供了前所未有的分辨率。高通量体内筛选加速了新的转移调节因子的系统鉴定,人源化小鼠模型为研究人类特异性肿瘤免疫相互作用和支持免疫疗法的临床前评估提供了临床相关的系统。总的来说,这些临床前系统正在重塑我们对SCLC转移的理解,并为指导治疗发现提供了强大的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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